Jedrzejowska H - Search Results

1

Focally folded myelin in Charcot-Marie-Tooth type 1B disease is associated with Asn131Lys mutation in myelin protein zero gene: short report.

Kochański A, Drac H, Jedrzejowska H, Hausmanowa-Petrusewicz I. Kochański A, et al. Among authors: jedrzejowska h. Eur J Neurol. 2003 Sep;10(5):547-9. doi: 10.1046/j.1468-1331.2003.00640.x. Eur J Neurol. 2003. PMID: 12940837

2

Uncompacted myelin in hereditary neuropathy with liability to pressure palsies with the 17 p11.2 deletion.

Jedrzejowska H, Fidziańska A, Kochański A. Jedrzejowska H, et al. Folia Neuropathol. 1999;37(4):220-6. Folia Neuropathol. 1999. PMID: 10705641

3

[Charcot-Marie Tooth type X (CMTX) disease: clinical and genetic characteristics of eleven patients].

Kochański A, Ryniewicz B, Jedrzejowska H, Kabzińska D. Kochański A, et al. Among authors: jedrzejowska h. Neurol Neurochir Pol. 2002 Nov-Dec;36(6):1087-94. Neurol Neurochir Pol. 2002. PMID: 12715686 Polish.

4

Mutation screening of Charcot-Marie-Tooth patients in Poland.

Kochański A, Timmerman V, Jedrzejowska H, Ryniewicz B, Löfgren A, De Vriendt E, Van Broeckhoven C, Latos-Bieleńska A, Hausmanowa-Petrusewicz I. Kochański A, et al. Among authors: jedrzejowska h. Ann N Y Acad Sci. 1999 Sep 14;883:493-6. Ann N Y Acad Sci. 1999. PMID: 10586282 No abstract available.

5

A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth disease.

Kochanski A, Lofgren A, Jedrzejowska H, Ryniewicz B, Czarny-Ratajczak M, Barciszewska A, Samocko J, Hausmanowa-Petrusewicz I, De Jonghe P, Timmerman V, Latos-Bielenska A. Kochanski A, et al. Among authors: jedrzejowska h. Hum Mutat. 2001 Feb;17(2):157. doi: 10.1002/1098-1004(200102)17:2<157::AID-HUMU22>3.0.CO;2-E. Hum Mutat. 2001. PMID: 11180613 No abstract available.

6

Mutation Screening of Charcot-Marie-Tooth Patients in Poland.

Kochański A, Timmerman V, Jedrzejowska H, Ryniewicz B, Löfgren A, De Vriendt E, VAN Broeckhoven C, Latos-Bieleńska A, Hausmanowa-Petrusewicz I. Kochański A, et al. Among authors: jedrzejowska h. Ann N Y Acad Sci. 1999 Oct;883(1):493-496. doi: 10.1111/j.1749-6632.1999.tb08619.x. Ann N Y Acad Sci. 1999. PMID: 29086975 No abstract available.

7

[Genotype-phenotype correlation in hereditary motor-sensory neuropathy type IA associated with duplication in chromosome 17p11.2-12].

Ryniewicz B, Jedrzejowska H, Kochański A. Ryniewicz B, et al. Among authors: jedrzejowska h. Neurol Neurochir Pol. 2000 Nov-Dec;34(6):1145-53. Neurol Neurochir Pol. 2000. PMID: 11317491 Polish.

8

Nerve conduction in the Guillain-Barré-Strohl syndrome.

Hausmanowa-Petrusewicz I, Emeryk B, Rowińska-Marcińska K, Jedrzejowska H. Hausmanowa-Petrusewicz I, et al. Among authors: jedrzejowska h. J Neurol. 1979 May 2;220(3):169-84. doi: 10.1007/BF00705535. J Neurol. 1979. PMID: 88509

9

Familial neuropathy with liability to pressure palsies. Report of a case.

Jedrzejowska H, Hausmanowa-Petrusewicz I. Jedrzejowska H, et al. Ital J Neurol Sci. 1981 Aug;2(3):229-36. doi: 10.1007/BF02335402. Ital J Neurol Sci. 1981. PMID: 6281213

10

[Formation of "onion bulbs" in Charcot-Marie-Tooth and Dejerine-Sottas hypertrophic neuropathies].

Jedrzejowska H, Drac H, Sawicka E. Jedrzejowska H, et al. Neuropatol Pol. 1975 Jan-Mar;13(1):93-106. Neuropatol Pol. 1975. PMID: 1118064 Polish. No abstract available.

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